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Lack of correlation between the promastigote back-transformation assay and miltefosine treatment outcome
Author(s) -
Sarah Hendrickx,
Eline Eberhardt,
Annelies Mondelaers,
Suman Rijal,
Narayan Raj Bhattarai,
JeanClaude Dujardin,
Peter Delputte,
Paul Cos,
Louis Maes
Publication year - 2015
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dkv237
Subject(s) - miltefosine , amastigote , leishmaniasis , leishmania donovani , biology , drug resistance , visceral leishmaniasis , medicine , leishmania , immunology , microbiology and biotechnology , parasite hosting , world wide web , computer science
Widespread antimony resistance in the Indian subcontinent has enforced a therapy shift in visceral leishmaniasis treatment primarily towards miltefosine and secondarily also towards paromomycin. In vitro selection of miltefosine resistance in Leishmania donovani turned out to be quite challenging. Although no increase in IC50 was detected in the standard intracellular amastigote susceptibility assay, promastigote back-transformation remained positive at high miltefosine concentrations, suggesting a more 'resistant' phenotype. This observation was explored in a large set of Nepalese clinical isolates from miltefosine cure and relapse patients to assess its predictive value for patient treatment outcome.

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